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Symbol
Name
ID
Pex7
peroxisomal biogenesis factor 7
MGI:1321392
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Anosmia
Spasticity
Delayed CNS myelination
Sensorimotor neuropathy
Sensory impairment
Cerebral cortical atrophy
Increased CSF protein
Ataxia
Hyporeflexia
Intellectual disability
Seizures
Disease(s) Associated with PEX7
Refsum disease
rhizomelic chondrodysplasia punctata type 1

Mouse Phenotypes
abnormal neuronal migration
abnormal hippocampus morphology
abnormal cerebral cortex morphology
abnormal spinal cord morphology
demyelination
Availability Mouse Genotype
Pex7tm1Nbra/Pex7tm1Nbra
Pex7tm1Rjaw/Pex7tm1Rjaw

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
08/06/2019
MGI 6.14
The Jackson Laboratory